AstraZeneca

Associate Quality Control

US - Frederick - MD Full time

Associate Quality Control

Must be available to work 2nd Shift - Wednesday to Saturday, 2PM to Midnight

Job Responsibilities

  • Responsible for performing laboratory testing.
  • Assist with/ complete routine tests on products and materials and help generate laboratory results, under supervision.
  • Maintain lab from housekeeping and stocking perspective.
  • Perform appropriate tasks in the laboratory (e.g. sample prep, recording of results) to meet needs and demands of the work plan.
  • Set up and take down testing and other laboratory equipment and clean up the testing sites.
  • Identify and highlight equipment and testing issues.
  • Support with the availability of proper equipment and supplies for testing
  • Enters data evaluated for compliance to specifications and reports abnormalities.
  • Reads, understands, and follows SOP’s and complies with cGMP’s
  • Applies critical thought to solving problems.
  • Works on problems requiring an in-depth knowledge of scientific methods and techniques.
  • General supervision and  instructions given for routine work.  Detailed instructions given for new activities or special assignments.

Accountabilities

  • Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role.  Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time.   Report potential issues of non-compliance.
  • Ensure and monitor compliance by team members and third parties by (a) positively reinforcing the Code of Conduct and all relevant AstraZeneca Policies and Standards, (b) ensuring completion of all required training, (c) fostering a culture of openness in which employees are comfortable raising questions or concerns, and (d) immediately addressing and reporting, as appropriate, instances of non-compliance.
  • Manager Accountabilities at AstraZeneca include Ethical Conduct and Compliance, Team Management, Performance Management, Individual Development Planning, Talent Management, Recruitment, People information, SHE accountabilities, and Fiscal and Financial awareness. 
  • Leaders with accountability for GXP areas are expected to understand the legal and regulatory requirements of their roles in providing appropriate resources (which could be human, financial, material, facilities, and equipment) to maintain the Quality system and continually improve its effectiveness.

Essential Qualifications, Skills and Experience

  • High school diploma or equivalent or High school diploma or GED, with 4 years of experience
  • Associate's degree and 2 years of work experience
  • Bachelor’s degree and 0 years of experience

Desirable Qualifications, Skills and Experience

  • Bachelor’ degree in Scientific / Biotech / Pharmaceutical field of study, preferred 0-5 years experience

The annual base pay for this position ranges from $55,920 to $83,881. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

28-Apr-2026

Closing Date

11-May-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.